Molecular basis for treating endometriosis with aromatase inhibitors

被引:78
作者
Bulun, SE
Zeitoun, KM
Takayama, K
Sasano, H
机构
[1] Univ Illinois, Dept Obstet & Gynecol, Chicago, IL 60612 USA
[2] Univ Illinois, Dept Mol Genet, Chicago, IL 60612 USA
[3] Columbia Univ Coll Phys & Surg, Dept Obstet & Gynecol, New York, NY 10032 USA
[4] Tohoku Univ, Sch Med, Dept Pathol, Sendai, Miyagi 980, Japan
[5] Tohoku Univ, Sch Med, Dept Obstet & Gynecol, Sendai, Miyagi 980, Japan
关键词
aromatase; aromatase inhibitor; endometriosis; endometrium; oestrogen biosynthesis;
D O I
10.1093/humupd/6.5.413
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Although treatment of one unusually aggressive case of postmenopausal endometriosis with an aromatase inhibitor has been strikingly successful, large clinical trials are required to establish whether aromatase inhibitors will have a significant role in the medical management of endometriosis. Introduction of aromatase inhibitors into the treatment of endometriosis underscores the importance of basic research leading to the development of novel strategies in reproductive disorders. It was shown earlier that aromatase activity was not detectable in normal endometrium, Aromatase, however, is expressed inappropriately in endometriosis and stimulated by prostaglandin E-2. Aromatase activity gives rise to local biosynthesis of oestrogen, which, in turn, stimulates prostaglandin E-2 production, thus establishing a positive feedback cycle, This favours accumulation of oestrogen and prostaglandins in endometriosis, which is an inflammatory disorder dependent on oestrogen for growth.
引用
收藏
页码:413 / 418
页数:6
相关论文
共 34 条
[1]   AROMATIZATION OF ANDROSTENEDIONE BY HUMAN ADIPOSE-TISSUE STROMAL CELLS IN MONOLAYER-CULTURE [J].
ACKERMAN, GE ;
SMITH, ME ;
MENDELSON, CR ;
MACDONALD, PC ;
SIMPSON, ER .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1981, 53 (02) :412-417
[2]   Suppression of matrix metalloproteinases inhibits establishment of ectopic lesions by human endometrium in nude mice [J].
Bruner, KL ;
Matrisian, LM ;
Rodgers, WH ;
Gorstein, F ;
Osteen, KG .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (12) :2851-2857
[3]   CYP19 (AROMATASE CYTOCHROME-P450) GENE-EXPRESSION IN HUMAN-MALIGNANT ENDOMETRIAL TUMORS [J].
BULUN, SE ;
ECONOMOS, K ;
MILLER, D ;
SIMPSON, ER .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 79 (06) :1831-1834
[4]   EXPRESSION OF THE CYP19 GENE AND ITS PRODUCT AROMATASE CYTOCHROME-P450 IN HUMAN UTERINE LEIOMYOMA TISSUES AND CELLS IN CULTURE [J].
BULUN, SE ;
SIMPSON, ER ;
WORD, RA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1994, 78 (03) :736-743
[5]   A LINK BETWEEN BREAST-CANCER AND LOCAL ESTROGEN BIOSYNTHESIS SUGGESTED BY QUANTIFICATION OF BREAST ADIPOSE-TISSUE AROMATASE CYTOCHROME-P450 TRANSCRIPTS USING COMPETITIVE POLYMERASE CHAIN-REACTION AFTER REVERSE TRANSCRIPTION [J].
BULUN, SE ;
PRICE, TM ;
AITKEN, J ;
MAHENDROO, MS ;
SIMPSON, ER .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 77 (06) :1622-1628
[6]   PERITONEAL-MACROPHAGES FROM PATIENTS WITH ENDOMETRIOSIS RELEASE GROWTH-FACTOR ACTIVITY INVITRO [J].
HALME, J ;
WHITE, C ;
KAUMA, S ;
ESTES, J ;
HASKILL, S .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1988, 66 (05) :1044-1049
[7]   Immunolocalization and regulation of the chemokine RANTES in hunan endothelial and endometriosis tissues and cells [J].
Hornung, D ;
Ryan, IP ;
Chao, VA ;
Vigne, JL ;
Schriock, ED ;
Taylor, RN .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (05) :1621-1628
[8]   Interleukin-1β induces cyclooxygenase-2 gene expression in cultured endometrial stromal cells [J].
Huang, JC ;
Liu, DY ;
Yadollahi, S ;
Wu, KK ;
Dawood, MY .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (02) :538-541
[9]  
HUANG JC, 1996, P 52 ANN M AM SOC RE, V1
[10]   PHASE-I STUDY OF THE ORAL NONSTEROIDAL AROMATASE INHIBITOR CGS 20267 IN HEALTHY POSTMENOPAUSAL WOMEN [J].
IVESON, TJ ;
SMITH, IE ;
AHERN, J ;
SMITHERS, DA ;
TRUNET, PF ;
DOWSETT, M .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1993, 77 (02) :324-331